Issue 58, 2014

Propargylamine–isothiocyanate reaction: efficient conjugation chemistry in aqueous media

Abstract

A coupling reaction between secondary propargyl amines and isothiocyanates in aqueous media is described. The reaction is high-yielding and affords cyclized products within 2–24 h. A functionalized ether lipid was synthesized in 8 steps, formulated as liposomes with POPC and conjugated to FITC under mild conditions using this method.

Graphical abstract: Propargylamine–isothiocyanate reaction: efficient conjugation chemistry in aqueous media

Supplementary files

Article information

Article type
Communication
Submitted
01 Feb 2014
Accepted
28 May 2014
First published
29 May 2014

Chem. Commun., 2014,50, 7800-7802

Author version available

Propargylamine–isothiocyanate reaction: efficient conjugation chemistry in aqueous media

H. M.-F. Viart, T. S. Larsen, C. Tassone, T. L. Andresen and M. H. Clausen, Chem. Commun., 2014, 50, 7800 DOI: 10.1039/C4CC00863D

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements